BE809204A - Dihydroxy benzenes or their monoethers - from phenols or phenolic ethers, organic peracid plus specified catalyst for higher yields - Google Patents
Dihydroxy benzenes or their monoethers - from phenols or phenolic ethers, organic peracid plus specified catalyst for higher yieldsInfo
- Publication number
- BE809204A BE809204A BE139365A BE139365A BE809204A BE 809204 A BE809204 A BE 809204A BE 139365 A BE139365 A BE 139365A BE 139365 A BE139365 A BE 139365A BE 809204 A BE809204 A BE 809204A
- Authority
- BE
- Belgium
- Prior art keywords
- monoethers
- pref
- dihydroxy benzenes
- phenols
- higher yields
- Prior art date
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
Process for dihydroxy benzenes from hydroxybenzenes opt. substd. by 1-12C alkyl; and also for monoethers of dihydroxybenzenes from 1-12C alkyl or aryl phenolethers. The process is carried out, pref. at 50-100 degrees C, in the presence of one of: peracid stabilisers; N-contg. polycarboxylic acids able to chelate a heavy metal together with their Mg, Na, K salts; hydroxy polycarboxylic acids able to chelate with a heavy metal together with their Mg, Na salts; Na or K slats of phosphonic acid mono- or di-lower alkyl ethers; Na salt of pyrophosphoric acid mono-, di- or tri-lower alkyl ethers. Specif. using 2:6 di(hydroxymethyl)pyridine, 8-hydroxyquinoline, dioctyl dihydrogen pyraphosphates and pyrophosphates of formula H5R'5(P3O10)2 or Na5R'5(P3O10)2, where R' is 4-10C alkyl. Pref. peracids are peracetic, perpropionic or perisobutyric used at 0.1-0.5 mol/mol phenol. The catalyst is pref. 0.05-1% of the phenol wt. Process results in improved yields.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP47129301A JPS5210852B2 (en) | 1972-12-25 | 1972-12-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
BE809204A true BE809204A (en) | 1974-04-16 |
Family
ID=15006172
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE139365A BE809204A (en) | 1972-12-25 | 1973-12-27 | Dihydroxy benzenes or their monoethers - from phenols or phenolic ethers, organic peracid plus specified catalyst for higher yields |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS5210852B2 (en) |
BE (1) | BE809204A (en) |
-
1972
- 1972-12-25 JP JP47129301A patent/JPS5210852B2/ja not_active Expired
-
1973
- 1973-12-27 BE BE139365A patent/BE809204A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPS4986334A (en) | 1974-08-19 |
JPS5210852B2 (en) | 1977-03-26 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
RE | Patent lapsed |
Owner name: AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY & OX Effective date: 19871231 |